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Dicofol

CAS No. 115-32-2
Chemical Name: Dicofol
Synonyms: DTMC;fw293;Hifol;Carbax;FW 293;hilfol;Milbol;ACARIN;Akarin;Dichlo
CBNumber: CB8424167
Molecular Formula: C14H9Cl5O
Formula Weight: 370.49
MOL File: 115-32-2.mol
Dicofol Property
Melting point : 78.5°C
Boiling point : 225°C
density : 1.45
Fp : 11 °C
storage temp. : APPROX 4°C
Water Solubility : Slightly soluble. <0.01 g/100 mL at 22 ºC
Merck : 13,3113
Stability:: Stable. Combustible. Incompatible with strong oxidizing agents. Hydrolyzes in basic solution. Corrodes some metals.
CAS DataBase Reference: 115-32-2(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid, [3,5-diiodo-4-(4-hydroxy-3-iodophenoxy) phenyl]-, 2-[diethylamino]ethyl ester, hydrochloride(115-32-2)
EPA Substance Registry System: Benzenemethanol, 4-chloro-.alpha.-(4-chlorophenyl)-. alpha.-(trichloromethyl)- (115-32-2)
Safety
Hazard Codes : Xn;N,N,Xn,T,F
Risk Statements : 21/22-38-43-50/53-39/23/24/25-23/24/25-11
Safety Statements : 36/37-60-61-45-16-7
RIDADR : UN 2761/3077
RTECS : DC8400000
Hazardous Substances Data: 115-32-2(Hazardous Substances Data)

Dicofol Chemical Properties,Usage,Production

Chemical Properties
white or grey powder, or colourless crystals
Uses
Acaricide, organochlorine pesticide. Dicofol is a non-systemic acaricide/miticide currently registered in the US and Canada for use on a wide variety of crops.
General Description
Dicofol or kelthane is a white crystalline, wettable powder dissolved in a liquid carrier, (water). The primary hazard is the threat to the environment. Immediate steps should be taken to limit its spread to the environment. Since Dicofol is a liquid Dicofol can easily penetrate the soil and contaminate groundwater and nearby streams. Dicofol can cause illness by inhalation, skin absorption, and/or ingestion. Dicofol is used as a pesticide.
Air & Water Reactions
Hydrolyzed in alkaline media to dichlorobenzophenone and chloroform. Insoluble in water.
Reactivity Profile
Dicofol is an organochlorine bridged diphenyl. Halogenated aliphatic compounds are moderately or very reactive. Reactivity generally decreases with increased degree of substitution of halogen for hydrogen atoms. Halogenated aliphatics are incompatible with strong oxidizing and reducing agents. Also, they are incompatible with many amines, nitrides, azo/diazo compounds, alkali metals, and epoxides. Dicofol hydrolyzes in alkali. Dicofol is slightly corrosive to metals. Contact with steel at elevated temperatures causes formation of toxic gases. .
Health Hazard
Inhalation or ingestion causes nausea, headache, weight loss, convulsions, possible kidney and liver damage. Contact with eyes causes irritation.
Dicofol Preparation Products And Raw materials
Raw materials
Xylene p-Toluenesulfonic acid 2,2'-Azobis(2-methylpropionitrile) Iodic acid Methanesulfonic acid Chlorine 4,4'-DDT EMULSIFIER Sodium hydroxide Sulfuric acid
Preparation Products
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115-32-2(Dicofol)Related Search:
Etanol 4,4'-DDM 2,2,2-Trichloro-1-phenylethanol Chlorobutanol (S)-1-Chloro-2-propanol 4,4'-DICHLORO-ALPHA-METHYLBENZHYDROL 1,1'-(2,2,2-trichloroethylidene)dibenzene 2-CHLORO-1-(4-CHLORO-PHENYL)-ETHANOL 4,4'-DDT (S)-2-CHLORO-1-PHENYL-ETHANOL 1 -(4-CHLOROPHENYL)-1 -PHENYLETHANOL 2-(4-CHLOROPHENYL)ETHYL CHLORIDE (R)-4-CHLORO-ALPHA-METHYLBENZYL ALCOHOL 1,1,1-TRICHLORO-2-PROPANOL Dicofol 3-Chloropropyltrichlorosilane Trichloroacetyl chloride Dichloroacetic acid
1,1,1-Trichlor-2,2-bis(4-chlorphenyl)-aethanol 1,1-Bis(4-chlorophenyl)-2,2,2-trichloroethanol 2,2,2-Trichloor-1,1-bis(4-chloor fenyl)-ethanol 2,2,2-trichloor-1,1-bis(4-chloorfenyl)-ethanol 2,2,2-Trichlor-1,1-bis(4-chlor-phenyl)-aethanol 2,2,2-trichloro-1,1-bis(4-chlorophenyl)-ethanol(french) 2,2,2-Trichloro-1,1-bis(4-cloro-fenil)-etanolo 2,2,2-trichloro-1,1-bis(p-chlorophenyl)-ethano 2,2,2-trichloro-1,1-bis(p-chlorophenyl)ethanol 2,2,2-trichloro-1,1-di-(4-chlorophenyl)ethanol 2,2,2-Trichloro-1,1-di(4-chlorophenyl)ethanol 4,4’-dichloro-alpha-(trichloromethyl)-benzhydro 4,4’-dichloro-α-(trichloromethyl)benzhydrol 4-Chloro-(4-chlorophenyl)-(trichloromethyl)benzenemethanol 4-chloro-.alpha.-(4-chlorophenyl)-.alpha.-(trichloromethyl)-Benzenemethanol 4-chloro-alpha-(4-chlorophenyl)-alpha-(trichloromethyl)-benzenemethano 4-Chloro-alpha-(4-chlorophenyl)-alpha-(trichloromethyl)benzenemethanol 4-chloro-alpha-(4-chlorophenyl)-alpha-(trichloromethyl)benzylalcohol Benzenemethanol, 4-chloro-alpha-(4-chlorophenyl)-alpha-(trichloromethyl)- benzenemethanol,4-chloro-α-(4-chlorophenyl)-α-(trichloromethyl)- Benzhydrol, 4,4'-dichloro-alpha-(trichloromethyl)- benzhydrol,4,4’-dichloro-α-(trichloromethyl)- Carbax caswellnumber093 Decofol Dichlorokelthane dicofol,[liquid] dicofol,[solid] DTMC ENT 23,648 ent23,648 epapesticidechemicalcode010501 Ethanol, 2,2,2-Trichloro-1,1-bis(4-chlorophenyl)- Ethanol, 2,2,2-trichloro-1,1-bis(p-chlorophenyl)- Ethanol,1,1-bis(p-chlorophenyl)-2,2,2-trichloro- ethanol,2,2,2-trichloro-1,1-bis(4-chlorophenyl)- Fumite Dicofol FW 293 fw293 Hifol hilfol Hilfol 18.5 ec hilfol18.5ec Keltane Kelthane A Kelthane dust base kelthanea kelthanedustbase Kelthanethanol Kelthone Milbol NCI-C00486 p,p’-kelthane p,p-Dicofol p,p'-Kelthane para,para’-kelthane para,para'-Kelthane KELTHANE
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